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Complexity of Antibiotic Resistance in Commensal Escherichia coli Derived from Pigs from an Intensive-Production Farm

机译:共生大肠杆菌中抗生素抗性的复杂性来自猪的猪,源自强化生产农场

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Antibiotics in animal husbandry are used to maintain welfare, but had to the generation of resistant strains. We analyzed commensal multidrug-resistant Escherichia coli from pigs at the beginning and end of the production cycle in a farm with a farrow-to-finish system in order to investigate whether clonal spread or horizontal gene transfer constitutes the main factor responsible for the prevalence of resistance in this environment. Among 380 isolates, 56 multidrug-resistant E. coli with a similar resistant phenotype were selected for more detailed investigations including a genomic similarity analysis and the detection of mobile elements. Isolates carried bla(TEM-1), aadA1, strA/B, tetA , tetB, tetC, dfrA1, dfrA5, dfrA7, dfrA12, sul1 , suI2, sul3, and qnrS resistance genes, with the common co-occurrence of genes encoding the same resistance phenotype. A pulse-field gel electrophoresis analysis of the genomic similarity of multidrug-resistant E. coli showed &= 65% similarity of most of the tested strains and did not reveal a dominant clone responsible for the prevalence of resistance. Class 1 and 2 integrons and transposons 7 and 21 were detected among mobile elements; however, some were truncated. Plasmids were represented by 11 different incompatibility groups (K, FIB, I1, FIIA, FIC, FIA, Y, P, HI1, B/O, and T). Genetic resistance traits were unevenly spread in the clonal groups and suggested the major rearrangement of genetic material by horizontal gene transfer. The present results revealed that in commensal E. coli from pigs in a homogeneous farm environment, there was no dominant clone responsible for the spread of resistance and persistence in the population.
机译:畜牧业的抗生素被用来维持福利,但不得不产生抗性菌株。我们分析了在农场的生产周期开始和结束的猪中的共生多药抗性大肠杆菌,以便进行骚动到结束系统,以调查克隆扩散或水平基因转移是否构成了负责患病率的主要因素在这种环境中的抵抗力。在380个分离物中,选择具有类似抗性表型的56个多药物大肠杆菌以进行更详细的研究,包括基因组相似性分析和移动元件的检测。分离物携带的BLA(TEM-1),AADA1,Stra / B,TETA,TETB,TETC,DFRA1,DFRA5,DFRA7,DFRA12,SUL1,SUI2,SUL3和QNRS抗性基因,具有编码的共同的共同发生相同的抗性表型。多药物抗性大肠杆菌的基因组相似性的脉冲场凝胶电泳分析& LT; =大多数测试菌株的65%相似性,并且没有揭示负责抗性患病率的显性克隆。在移动元件中检测到1级和2级积分子和转座子7和21;但是,有些人被截断了。质粒由11种不同的不相容性基团(K,FIB,I1,菲亚,FIC,FIA,Y,P,HI1,B / O和T)表示。遗传性耐药性在克隆基团中不均匀地扩散,并提出了通过水平基因转移的主要重新排列遗传物质。目前的结果表明,在均匀农场环境中的猪的共和大肠杆菌中,没有主导克隆负责抗性和持续存在的群体。

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